Variant report
| Variant | rs8056389 |
|---|---|
| Chromosome Location | chr16:71589816-71589817 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr16:71585600-71591400 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
| 2 | chr16:71587000-71598000 | Weak transcription | Brain Anterior Caudate | brain |
| 3 | chr16:71588400-71592200 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
| 4 | chr16:71589000-71590200 | Enhancers | Primary monocytes fromperipheralblood | blood |
| 5 | chr16:71589000-71590400 | Strong transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
| 6 | chr16:71589000-71594800 | Enhancers | HepG2 | liver |
| 7 | chr16:71589400-71591800 | Weak transcription | Fetal Intestine Small | intestine |
| 8 | chr16:71589600-71591400 | Weak transcription | Fetal Intestine Large | intestine |
| 9 | chr16:71589800-71591600 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
